US5700598A - Method for preparing mixed amorphous vanadium oxides and their use as electrodes in reachargeable lithium cells - Google Patents
Method for preparing mixed amorphous vanadium oxides and their use as electrodes in reachargeable lithium cells Download PDFInfo
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- US5700598A US5700598A US08/678,210 US67821096A US5700598A US 5700598 A US5700598 A US 5700598A US 67821096 A US67821096 A US 67821096A US 5700598 A US5700598 A US 5700598A
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G31/00—Compounds of vanadium
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G51/00—Compounds of cobalt
- C01G51/006—Compounds containing, besides cobalt, two or more other elements, with the exception of oxygen or hydrogen
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- C—CHEMISTRY; METALLURGY
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- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G53/00—Compounds of nickel
- C01G53/006—Compounds containing, besides nickel, two or more other elements, with the exception of oxygen or hydrogen
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- C—CHEMISTRY; METALLURGY
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- C01P2002/00—Crystal-structural characteristics
- C01P2002/02—Amorphous compounds
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- C—CHEMISTRY; METALLURGY
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- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
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- C—CHEMISTRY; METALLURGY
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- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/40—Electric properties
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- Lithium ion secondary cells represent an economically important sector of the battery market.
- One commercially significant embodiment of such secondary cells employs a lithiated intercalation metal oxide as the positive electrode and a carbonaceous material as the negative electrode.
- lithiated intercalation metal oxide as the positive electrode
- carbonaceous material as the negative electrode.
- Commonly employed lithiated metal oxides include LiCoO 2 , LiNiO 2 , and LiMn 2 O 4 , of which LiCoO 2 is the most widely employed material.
- a common feature of all these lithiated metal oxides is that only about 0.5 lithium atoms per transition metal can be practically used in the charge/discharge cycles of the cells. Research investigations continue in a search for better, cheaper, and more efficient electrode materials.
- J. Dahn et al. attempted to improve the electrochemical characteristics of the carbonaceous material by means of pyrolytic processing of organic materials to obtain a carbonaceous electrode material.
- J. Dahn et al. Lithium batteries, (1994).
- F. Disma et al. has explored mechanical processing of the negative electrode material so as to augment its electrochemical capacity. Unfortunately, these approaches have not proved significantly successful.
- It is another object of the present invention to provide a novel method for preparing an amorphous binary non-lithiated vanadium metal oxide of the formula M y V z O.sub.(5z+ny)/2, where M is a metal, 0 ⁇ y ⁇ 3, 1 ⁇ z ⁇ 4, and n 2 or 3, which yields the binary non-lithiated vanadium metal oxide in an amorphous form by means of a simple, efficient synthesis.
- It is a still further object of the present invention to provide a rechargeable lithiated intercalation battery cell comprising a positive electrode, a negative electrode, and an electrolyte, wherein the active material of the negative electrode is an amorphous ternary lithiated vanadium metal oxide of the formula Li x M y V z O.sub.(x+5z+ny)/2 or an amorphous binary non-lithiated vanadium metal oxide of the formula M y V z O.sub.(5z+ny)/2, prepared according to the methods of the present invention.
- a non-aqueous secondary cell comprising an active negative electrode material, an active positive electrode material and an non-aqueous electrolyte
- said amorphous ternary lithiated vanadium metal oxide prepared by a process comprising the steps of creating an aqueous solution of at least one metavanadate salt selected from the group consisting of NH 4 VO 3 and NaVO 3 , and a nitrate salt of the formula M(NO 3 ) n , containing a large excess of a lithium salt; heating the solution; adding a sufficient amount of a base to obtain a pH greater than 8; and precipitating the a
- a non-aqueous secondary cell comprising an active negative electrode material, an active positive electrode material and an non-aqueous electrolyte
- FIG. 1 depicts the respective X-ray diffraction traces of amorphous and crystalline Li x NiVO 4 prepared according to the present invention
- FIGS. 2 and 3 respectively depict the voltage/lithium content curve and the capacity/cycle number curve of a cell employing amorphous Li x NiVO 4 as the active positive electrode material v. Li;
- FIGS. 4 and 5 respectively depict the voltage/lithium content curve and the capacity/cycle number curve of a cell employing crystalline Li x NiVO 4 as the active positive electrode material v. Li;
- FIGS. 6 and 7 respectively depict the voltage/lithium content curve and the capacity/cycle number curve of a cell employing Li x NiVO 4 , re-amorphized by mechanical grinding, as the active positive electrode material v. Li;
- FIG. 8 depicts the respective X-ray diffraction traces of amorphous and crystalline InVO 4 prepared according to the present invention
- FIGS. 9 and 10 depict the voltage versus lithium content curves for cells employing InVO 4 as the active positive electrode material v. Li and cycled, respectively, with varying relaxation times;
- FIG. 11 depicts the voltage versus lithium content curve for a Li-ion cell employing InVO 4 prepared according to the present invention as the active negative electrode material v. Li x Mn 2 O 4 .
- vanadium oxides for graphite as the negative electrode in rechargeable lithium ion cells results in a reduction of cell output voltage.
- the average voltage at which these vanadium oxide-based materials intercalate lithium ions is about 1.4 V, as compared an intercalation voltage of about 0.3 V for a conventional graphite negative electrode.
- vanadium oxides can reversibly intercalate up to about 7 lithium ions per unit formula, resulting in energy densities of about 800 to 900 Ah/kg, which is about two to two-and-one-half times greater than the energy density of the conventional graphite electrodes. Because of this greater electrochemical capacity of the lithiated vanadium oxides, the energy density of a rechargeable lithium ion cell employing a vanadium oxide as the negative electrode is equivalent to that achieved with a graphite negative electrode, within ⁇ 5%.
- vanadium oxide-based materials One peculiar feature of the vanadium oxide-based materials is a propensity to become amorphous upon lithium intercalation/deintercalation, as previously demonstrated by Delmas et al., J. Power Sources, 34, 103 (1991).
- V 2 O 5 below 1 V
- a substantial change was observed in the electrochemical potential relative to the lithium content in Li x V 2 O 5 between the first and second discharge.
- a stepwise voltage variation was seen during the initial discharge, while a smooth and continuous variation in voltage relative to lithium content was found with the second discharge.
- vanadium metal oxides it is suggested that this amorphization is a result of the tendency of a vanadium ion to alter its coordination sphere upon reduction.
- vanadium in LiNiVO 4 , vanadium is in the +5 oxidation state and possesses a tetrahedral geometry.
- the V +4 ion prefers an octahedral coordination sphere as a result of crystal field stabilization. This shift in coordination geometry results in local structural modification. It is believed that the amorphization observed during electrochemical cycling results from such changes in coordination geometry, associated with the reduction in the vanadium oxidation state.
- LiMVO 4 -based electrodes where M is a metal selected from the group of cadmium, cobalt, zinc, nickel, copper, and magnesium
- M is a metal selected from the group of cadmium, cobalt, zinc, nickel, copper, and magnesium
- lithiated vanadium metal oxide compositions in an amorphous state.
- these materials had been prepared by reacting stoichiometric amounts of lithium carbonate (Li 2 CO 3 ), NH 4 VO 3 and M(NO 3 ) 2 , (where M is a metal selected from the group of cadmium, cobalt, zinc, nickel, copper, and magnesium) at 500° C. for 48 hours.
- some synthetic methods provided crystalline lithiated vanadium metal oxide compositions, which had to be further processed by means of an amorphization step. Such syntheses are time-consuming, energy-inefficient, and labor-intensive. There remains a need for an efficient and effective method for preparing amorphous LiMVO 4 .
- lithiated vanadium metal oxides have generated such significant enthusiasm and widespread research interest regarding their use in lithiated intercalation cells, researchers have focused their attention on the development of effective techniques for manufacturing these compounds.
- Conventional fabrication of lithiated vanadium oxides requires calcination and annealing at temperatures greater than 500° C. for a period of a several days, a technique which is costly and inefficient.
- a new method for producing lithiated vanadium metal oxides of controlled morphology and grain size was sought so as to improve the electrochemical performance of the oxides.
- amorphous LiNiVO 4 was then obtained by further adjusting the pH to a value in the range of about 8.0 to about 9.0, preferably to about 8.5, by the addition of an appropriate base such as NH 4 OH or organic bases.
- Suitable bases include ammonia; amines; alkali hydroxides, including lithium hydroxide. These bases can be added directly or as aqueous solutions of the base.
- amorphous LiNiVO 4 can be prepared by a method which does not require calcination and annealing at temperatures greater than 500° C. for a period of a several days. They have found that amorphous lithiated vanadium metal oxides can be prepared by means of a low temperature synthesis, comprising creating an aqueous solution of at least one metavanadate salt selected from the group consisting of NH 4 VO 3 and NaVO 3 , and a nitrate salt of the formula M(NO 3 ) n , containing a large excess of a lithium salt; heating the solution; adding a sufficient amount of a base to obtain a pH greater than 8; and precipitating the amorphous lithiated vanadium metal oxide.
- this method is not limited to amorphous lithiated vanadium metal oxides, but, rather, can be used to prepare amorphous vanadium oxide-based compounds.
- Ammonium metavanadate (NH 4 VO 3 ) was initially dissolved in water by heating and stirring to yield a solution of about 2.5 ⁇ 10 -2 M.
- a separate solution of Ni(NO 3 ) 2 /LiNO 3 in the ratio of about 1:15 was prepared such that the separate solution had a concentration of Ni(NO 3 ) 2 of about 4.5 ⁇ 10 -2 M. and a concentration of LiNO 3 of about 0.7M.
- the cold solution of nitrate salts was added.
- the pH of the resultant solution was 5 and no precipitation occurred.
- the solution was heated (80° C. to 90° C.) and stirred, the pH was adjusted to 8.5 by means of a 3N ammoniacal solution. A yellow precipitate appeared spontaneously.
- the mixture continued to be stirred and heated for about 10 minutes.
- Filtration of the precipitate was carried out with a 0.1 ⁇ m filter.
- the precipitate can be separated from the filtrate by means of centrifugation.
- the solid precipitate which was yellow-green in color, was then washed sequentially with water and ethanol to entrain and remove NH 3 .
- the precipitate was then dried in a 50° C. oven for about 12 hours.
- X-ray diffraction analysis of the solid indicated that the lithiated vanadium metal oxide was amorphous, as shown by the relatively featureless trace 12 in FIG. 1.
- the sample was then heated at 300° C. for about 10 hours during which crystallization developed, as was confirmed in trace 16 of subsequent room temperature X-ray analysis.
- the specific surface area of both the amorphous lithiated vanadium nickel oxide and the crystallized lithiated vanadium nickel oxide were measured, with the amorphous material having a specific surface area of about 30 to 36 m 2 /g and the crystalline material (annealed at 700° C.) having a specific surface area of about 3 to 4 m 2 /g.
- a rechargeable lithium cell using the amorphous lithiated vanadium oxide LiNiVO 4 of Example 1 as the active material of the positive electrode and lithium metal as the active material of the negative electrode was constructed in a Swagelock-type assembly.
- the positive electrode was prepared from a 0.3 mm thick film of 6 parts by weight of carbon black and 56 parts of LiNiVO 4 intimately dispersed in a binder matrix of 16 parts of an 88:12 vinylidene fluoride:hexafluoropropylene (PVDF:HFP) copolymer and 16 parts of compatible dibutylphthalate (DBP) plasticizer.
- a disk of 1 cm 2 was cut from the film and immersed in diethyl ether to extract substantially all the DBP plasticizer from the electrode composition.
- the DBP-free positive electrode disk after drying under vacuum for 1 hour, was placed in a dry box under a helium atmosphere.
- the negative electrode of the same size was prepared from a lithium metal foil pasted onto a nickel disk.
- the positive and negative electrodes were electrically isolated by a separator disk cut from a silica fiber mat, and soaked in an electrolyte solution of 1M LiPF 6 in an solvent mixture of 1/3 dimethyl carbonate and 2/3 ethylene carbonate.
- the cell assembly was then inserted into Swagelock hardware where physical contact between the cell components was ensured by spring pressure while the cell was maintained air-tight by stainless steel plungers.
- the cell was then removed from the dry box for electrochemical testing over a number of charge/discharge cycles between 0.05 V and 3 V by means of a MacPile system operating in a galvanostatic mode.
- FIGS. 2 and 3 respectively depict the voltage/lithium content curve and the capacity/cycle number curve for the amorphous Li x NiVO 4 cell.
- FIGS. 4 and 5 respectively illustrate the voltage/lithium content curve and the capacity/cycle number of the cell. With both cells, about 7 lithium ions per unit formula can be reversibly intercalated. However, the initial capacity achieved with amorphous Li x NiVO 4 is larger than that obtained with crystalline Li x NiVO 4 , resulting in capacities for cells employing amorphous Li x NiVO 4 as large as 920 mAh/g, about 2.5 times greater that obtained with a conventional graphite electrode.
- the method of the present invention it is not necessary to slowly transform the crystallized phase into an unordered amorphous phase.
- the desired ternary lithiated vanadium metal oxide is produced directly in an efficient and effective synthesis, in contrast to the time-consuming, energy-inefficient, and labor-intensive conventional process.
- these graphs indicate that the amorphous phase can reversibly intercalate as many lithium ions as the crystallized phase, but at a faster rate.
- FIGS. 6 and 7 respectively depict the voltage/lithium content curve and the capacity/cycle number curve for the resulting cell.
- the slight increase in the irreversible loss of capacity observed between the first discharge and first charge of a cell containing the re-amorphized Li x NiVO 4 is consistent with the small increase in specific surface area observed with the re-amorphized sample (6 m 2 /g) relative to the specific surface area of the crystallized sample (3 m 2 /g). Further, the irreversible loss of capacity between the first discharge and the first charge supports the hypothesis that such capacity loss occurs by means of a catalytic decomposition of the electrolyte on the surface of the metal oxide. It is also to be noted that the first discharge voltage is greater for the amorphous phase than for the crystallized phase. This observation is again consistent with the larger degree of amorphization. As the degree of disorder in the structure increases, the Fermi level rises in energy, resulting in an increase in the intercalation voltage.
- the observed capacity of the amorphous Li x NiVO 4 -based cell remains more constant than the capacity of the crystalline Li x NiVO 4 -based cell. Moreover, the capacity does not increase as had previously been observed with the crystalline lithiated vanadium oxides. It is believed that this constant capacity is a direct result of the initial amorphous character of the lithiated vanadium metal oxide produced by the process of the present invention, in contrast to the cycling that is required with the conventional syntheses of the crystalline lithiated vanadium oxide to achieve the proper degree of amorphization.
- Example 2 A process analogous to that of Example 1 was employed in the synthesis of LiCoVO 4 .
- Ammonium metavanadate (NH 4 VO 3 ) was initially dissolved in water with heating and stirring to yield a solution of about 2.5 ⁇ 10 -2 M.
- a separate solution of Co(NO 3 ) 2 /LiNO 3 in a ratio of about 1:20 was prepared such that the separate solution had a Co(NO 3 ) 2 concentration of about 4.5 ⁇ 10 -2 M and a LiNO 3 concentration of about 0.7M.
- the cold solution of nitrate salts was added.
- the pH of the resultant mixture was 5 and no precipitation occurred. While the solution was heated to a temperature of about 80° C. to 90° C.
- the analogous vanadium oxide Ni 3 (VO 4 ) 2 was obtained when the Li/Ni ratio was zero or insufficient. Therefore, the structures are different for LiNiVO 4 and Ni 3 (VO 4 ) 2 .
- Ni 2 V 2 O 7 was obtained.
- the pH of the solution containing Ni(NO 3 ) 2 and NH 4 VO 3 must be initially decreased to 2 by means of concentrated acid, for example HNO 3 . Afterwards, the pH is raised to a range of about 4 to about 5 so as to induce precipitation. During the initial pH adjustment from about 5 to about 2, the solution remained translucent. After washing and filtration, X-ray diffraction analysis of the resultant solid indicated that the solid phase was amorphous. Successive annealings of the solid precipitate did not progress towards crystallization as clearly as with Ni 3 (VO 4 ) 2 and LiNiVO 4 .
- Binary non-lithiated vanadium oxides of the formula M y V z O.sub.(5z+ny)/2, where M is a metal selected from the group of manganese, cobalt, iron, nickel, copper, cadmium, chromium, magnesium, aluminum, and indium, 0 ⁇ y ⁇ 3, 1 ⁇ z ⁇ 4, and n 2 or 3; MVO 4 , can be obtained by analogous aqueous syntheses.
- a solution of about 2.5 ⁇ 10 -2 M NH 4 VO 3 was mixed with a solution of about 4.5 ⁇ 10 -2 M In(NO 3 ) 3 .5H 2 O.
- the pH of the resultant solution was about 2 to about 2.5.
- Instantaneously upon mixing a precipitate was observed.
- the precipitate was redissolved by lowering the pH of the solution to about 1 with the addition of aliquots of 3N HNO 3 .
- the pH of the solution was then raised to about 4 by gently adding 3N NH 4 OH, at which pH the amorphous inVO 4 precipitated.
- Swagelock test cells were prepared as in Example 2 employing the amorphous InVO 4 as the active positive electrode material. Resulting cells were likewise tested in the MacPile system at a C/4 rate with a variation in relaxation time between charge and discharge cycles of 0.003 hours and 0.25 hours. The voltage/lithium content curves for such cell tests over the first 10 cycles are shown, respectively, in FIGS. 9 and 10. In both cases an irreversible component of self-discharge corresponding to about 3 lithium atoms per formula unit and a reversible component of self-discharge of about 6 lithium atoms per formula unit were observed. These results correlate with an initial capacity of about 900 mAh/g and represent the first time that lithium intercalation into an amorphous non-lithiated vanadium oxide has been achieved.
- a positive electrode was prepared as described in the noted patent in the form of a 0.2 mm thick film of 56 parts by weight of finely-divided LiMn 2 O 4 , 6 parts of carbon black, 15 parts of the PVdF:HFP copolymer, and 23 parts of DBP plasticizer.
- An electrolyte/separator film according to the patent was formed as a 85 ⁇ m thick film of the copolymer mixed with equal parts of DBP. The films were then assembled with the separator between the electrode components and the assembly was laminated with heat and pressure.
- a 1 cm 2 disk was cut from the laminate and immersed in diethyl ether to extract a substantial portion of the DBP plasticizer, and the disk was then immersed in the electrolyte solution of Example 2 which was absorbed into the copolymer matrix to activate the cell.
- the cell was then mounted in a Swagelok apparatus and tested in cycling between 4.5 V and 2 V with a current density of 350 mA/cm 2 . The results of such cycling are shown in FIG. 11.
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Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
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US08/678,210 US5700598A (en) | 1996-07-11 | 1996-07-11 | Method for preparing mixed amorphous vanadium oxides and their use as electrodes in reachargeable lithium cells |
AU36443/97A AU715258B2 (en) | 1996-07-11 | 1997-06-27 | A method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
EP97933196A EP0913007A1 (en) | 1996-07-11 | 1997-06-27 | A method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
JP10506049A JP2000503622A (en) | 1996-07-11 | 1997-06-27 | Method for producing mixed amorphous vanadium oxide and its use as electrode in rechargeable lithium batteries |
CA002259590A CA2259590C (en) | 1996-07-11 | 1997-06-27 | A method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
PCT/US1997/011285 WO1998002929A1 (en) | 1996-07-11 | 1997-06-27 | A method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
IL12770797A IL127707A (en) | 1996-07-11 | 1997-06-27 | Method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
MYPI97003089A MY133690A (en) | 1996-07-11 | 1997-07-08 | A method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
IDP972381A ID17594A (en) | 1996-07-11 | 1997-07-10 | METHOD OF MAKING A MIXTURE OF AMORF VANADIUM OXIDES AND ITS USE AS ELECTRODE ON LITIUM CELLS THAT CAN BE RE-FILLED |
TW086109800A TW362296B (en) | 1996-07-11 | 1997-07-11 | A method for preparing mixed amorphous vanadium oxides and their use as electrodes in rechargeable lithium cells |
JP2002242077A JP2003142096A (en) | 1996-07-11 | 2002-08-22 | Nonaqueous secondary battery |
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US08/678,210 US5700598A (en) | 1996-07-11 | 1996-07-11 | Method for preparing mixed amorphous vanadium oxides and their use as electrodes in reachargeable lithium cells |
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US (1) | US5700598A (en) |
EP (1) | EP0913007A1 (en) |
JP (2) | JP2000503622A (en) |
AU (1) | AU715258B2 (en) |
CA (1) | CA2259590C (en) |
ID (1) | ID17594A (en) |
IL (1) | IL127707A (en) |
MY (1) | MY133690A (en) |
TW (1) | TW362296B (en) |
WO (1) | WO1998002929A1 (en) |
Cited By (33)
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US5980855A (en) * | 1998-05-26 | 1999-11-09 | Rentech, Inc. | Method for preparing lithiated metal oxides |
US6017654A (en) * | 1997-08-04 | 2000-01-25 | Carnegie Mellon University | Cathode materials for lithium-ion secondary cells |
US6267943B1 (en) | 1998-10-15 | 2001-07-31 | Fmc Corporation | Lithium manganese oxide spinel compound and method of preparing same |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4675260A (en) * | 1984-11-12 | 1987-06-23 | Nippon Telegraph And Telephone Corporation | Lithium battery including vanadium pentoxide base amorphous cathode active material |
US5039582A (en) * | 1989-04-12 | 1991-08-13 | Consiglio Nazionale Delle Ricerche | High energy and high power lithium storage batteries, and method for producing the same |
US5284721A (en) * | 1990-08-01 | 1994-02-08 | Alliant Techsystems Inc. | High energy electrochemical cell employing solid-state anode |
US5334334A (en) * | 1993-03-30 | 1994-08-02 | Valence Technology, Inc. | Method of preparing lithium battery electrode compositions |
US5453337A (en) * | 1991-12-13 | 1995-09-26 | Centre National D'etudes Spatiales | Use of vanadium oxide and/or aluminum bronzes as a cathode material in electrochemical generators |
US5498494A (en) * | 1993-05-25 | 1996-03-12 | Wilson Greatbatch Ltd. | Preparation of silver vanadium oxide cathodes using AG20 and V205 as starting materials |
-
1996
- 1996-07-11 US US08/678,210 patent/US5700598A/en not_active Expired - Lifetime
-
1997
- 1997-06-27 EP EP97933196A patent/EP0913007A1/en not_active Withdrawn
- 1997-06-27 WO PCT/US1997/011285 patent/WO1998002929A1/en not_active Application Discontinuation
- 1997-06-27 CA CA002259590A patent/CA2259590C/en not_active Expired - Fee Related
- 1997-06-27 JP JP10506049A patent/JP2000503622A/en active Pending
- 1997-06-27 IL IL12770797A patent/IL127707A/en not_active IP Right Cessation
- 1997-06-27 AU AU36443/97A patent/AU715258B2/en not_active Ceased
- 1997-07-08 MY MYPI97003089A patent/MY133690A/en unknown
- 1997-07-10 ID IDP972381A patent/ID17594A/en unknown
- 1997-07-11 TW TW086109800A patent/TW362296B/en active
-
2002
- 2002-08-22 JP JP2002242077A patent/JP2003142096A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4675260A (en) * | 1984-11-12 | 1987-06-23 | Nippon Telegraph And Telephone Corporation | Lithium battery including vanadium pentoxide base amorphous cathode active material |
US5039582A (en) * | 1989-04-12 | 1991-08-13 | Consiglio Nazionale Delle Ricerche | High energy and high power lithium storage batteries, and method for producing the same |
US5284721A (en) * | 1990-08-01 | 1994-02-08 | Alliant Techsystems Inc. | High energy electrochemical cell employing solid-state anode |
US5453337A (en) * | 1991-12-13 | 1995-09-26 | Centre National D'etudes Spatiales | Use of vanadium oxide and/or aluminum bronzes as a cathode material in electrochemical generators |
US5334334A (en) * | 1993-03-30 | 1994-08-02 | Valence Technology, Inc. | Method of preparing lithium battery electrode compositions |
US5498494A (en) * | 1993-05-25 | 1996-03-12 | Wilson Greatbatch Ltd. | Preparation of silver vanadium oxide cathodes using AG20 and V205 as starting materials |
Non-Patent Citations (12)
Title |
---|
Bhattacharya et al., Solid State Communications, vol. 91, No. 5 pp. 357 360, Low Temperature Synthesis of a Bismuth Vanadium Oxide Isomorphous with B4V2011 (month unknown), 1994. * |
Bhattacharya et al., Solid State Communications, vol. 91, No. 5 pp. 357-360, "Low Temperature Synthesis of a Bismuth Vanadium Oxide Isomorphous with B4V2011" (month unknown), 1994. |
Chemical Abstracts Accession No. 105:899960 CA, Toboul et al. J. Therm. Anal. (1986), 31(1) 117 124 (month unknown), 1986. * |
Chemical Abstracts Accession No. 105:899960 CA, Toboul et al. J. Therm. Anal. (1986), 31(1) 117-124 (month unknown), 1986. |
Myazaki et al., CA Accession No. 112: 81039 "Secondary lithium batteries", JP 012654456, Oct. 1989. |
Myazaki et al., CA Accession No. 112: 81039 Secondary lithium batteries , JP 012654456, Oct. 1989. * |
Prokupkova et al., J. Materials Science, 31 (1996) 3391 3395 (month unavailable), 1996. * |
Prokupkova et al., J. Materials Science, 31 (1996) 3391-3395 (month unavailable), 1996. |
Sigala et al., "Amorphous lithium metal vanadium oxide compounds . . . ", CA Accession No. 125:304946, FR 2725709, Apr. 19, 1996. |
Sigala et al., "Synthesis and performances of new negative electrode materials . . . ", CA Accession No. 123:61226, Inst. Mater. Nantes, Nantes, 44072, Fr. C.R. Acad.Sci., Ser.II: Mec., Phys., Chim., Astron. (1995), 320 (10), 523-9(month unavailable), 1995. |
Sigala et al., Amorphous lithium metal vanadium oxide compounds . . . , CA Accession No. 125:304946, FR 2725709, Apr. 19, 1996. * |
Sigala et al., Synthesis and performances of new negative electrode materials . . . , CA Accession No. 123:61226, Inst. Mater. Nantes, Nantes, 44072, Fr. C.R. Acad.Sci., Ser.II: Mec., Phys., Chim., Astron. (1995), 320 (10), 523 9(month unavailable), 1995. * |
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Also Published As
Publication number | Publication date |
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TW362296B (en) | 1999-06-21 |
JP2003142096A (en) | 2003-05-16 |
WO1998002929A1 (en) | 1998-01-22 |
MY133690A (en) | 2007-11-30 |
JP2000503622A (en) | 2000-03-28 |
IL127707A (en) | 2002-05-23 |
IL127707A0 (en) | 1999-10-28 |
AU3644397A (en) | 1998-02-09 |
CA2259590A1 (en) | 1998-01-22 |
ID17594A (en) | 1998-01-15 |
AU715258B2 (en) | 2000-01-20 |
EP0913007A1 (en) | 1999-05-06 |
CA2259590C (en) | 2005-10-25 |
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